Journal of Bacteriology · 1976 · 62 citations · 48 references
Murein HydrolasesCellular EnzymologyBiochemistryCell DivisionProtein FoldingNatural SciencesMedicineEnzyme CatalysisMolecular BiologyEnzyme SpecificityCell Division CycleStructure-function Enzyme KineticsEscherichia Coli K-12Cellular BiochemistryProteomicsEnzymatic ModificationSoluble EnzymeBug 6
The specific activities of three murein hydrolases, carboxypeptidase I, carboxypeptidase II, and amidase were studied with respect to cell division in toluene-treated cells of Escherichia coli K-12. Carboxypeptidase I and amidase activities were constant throughout the division cycle in cells of D11/lac+pro+. Detectable carboxypeptidase II activity varied and was highest at the time of division by a factor of three. Carboxypeptidase II specific activity was also correlated with cell division in BUG 6, a temperature-sensitive mutant (J.N Reeve, D.J. Groves, and D.J. Clark, 1970). Fifteen minutes after shifting BUG 6 from 42 C (nondividing conditions) to 32 C (dividing conditions), there was a rapid resumption of cell division, accompanied by a 10-fold increase in the specific activity of carboxypeptidase II. These results demonstrate a correlation between detectable carboxypeptidase II activity and cell division as reflected by activity in toluene-treated cells. The subcellular location of carboxypeptidase II, a soluble enzyme was found to be periplasmic since it was released by tris(hydroxymethyl)-aminomethane-ethylenediaminetetraacetate treatment and osmotic shock, two methods known to release periplasmic enzymes.
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Transduction of linked genetic characters of the host by bacteriophage P1
E. S. Lennox · Virology · 1955 · 2.6K citations
Bacteriophage P1, Medicine, Genetics +12
V Braun, Kurt Rehn · European Journal of Biochemistry · 1969 · 540 citations · Full text
Membrane Structure, Proteinlipid Interaction, Protein Secretion +20